Acceleration of free release static coating of capillary columns by the presence of polar solvents in the coating solution – a theoretical study

The cause of an observed acceleration in the free release static coating process of a capillary when more polar solvents are added to alkanes as stationary phase solvents has been studied. By using a computer program, 9 of the relevant physical parameers were calculated in relation to the composition of the solvent hixtures. Curves of these parameters vs composition of the mixures were drawn. From the results it can be deduced that the change of these parameters with the increase of polar solvents in the solution, is probably insufficient to explain the drastic increase of the free release static coating speed. A physical model is proposed to calculate the depth of the meniscus around which sufficient heat can be transferred into the evaporating surface per unit time, to evaporate the solvent at a rate that the coating speed indicates. It is demonstrated that when pentane-acetone mixtures are used to coat a capillary, the depth of the meniscus indeed is greater than when pure pentane is used. The proposed model may lead to a better understanding of phenomena involved in the static coating process.     

212Th,a new isotope

The new isotope²¹²Th has been found to decay withE _α = (7.802 ±0.010) MeV andt _1/2 =(30 _?10 ⁺²⁰ ms. The decay energies of the previously observed isotopes²¹³Th and²¹⁴Th could be confirmed. The measured half-lives are in agreement with calculated values.     

The mechanism of long-range exciton diffusion in a nematically organized porphyrin layer

The exciton diffusion length in a nematically organized meso-tetra(4-n-butylphenyl)porphyrin (TnBuPP) layer was found to exceed 40 nm at a temperature of 90 K and to be equal to 22 +/- 3 nm at 300 K. The exciton diffusion coefficient decreases from > or = 3.1 x 10(-6) m(2)/s at 90 K to (2.5 +/- 0.5) x 10(-7) m(2)/s at 300 K. This thermal deactivation is attributed to exciton motion via a band mechanism. The motion of an exciton is not limited by polaronic effects; that is, the deformation of the atomic lattice around the exciton. The absence of polaronic self-trapping implies that the exciton diffusion coefficient can be enhanced by improvement of structural order and rigidity of the material.     

Evaluation of a dedicated gas chromatography-mass spectrometry method for the analysis of phenols in water

The increasing need to routinely analyse phenolic hydrocarbons in aqueous samples was addressed by the development and implementation of a state-of-the-art, though relatively straightforward, analytical procedure. The proposed method is based on acetic anhydride derivatisation of the native phenols, liquid-liquid extraction of the corresponding phenyl acetate esters and subsequent analysis by GC-MS. The key feature and main strength of the method is located at the injection step which applies 'at-once' large volume injection with a programmable temperature vaporizer (PTV)-type injector. In the proposed method, the sensitivity gain inherent to the higher injection volume was used entirely to proportionally miniaturize, considerably accelerate and effectively simplify the otherwise tedious and time-consuming derivatisation/extraction step. Method performance, as expressed in terms of repeatability, reproducibility, linearity and accuracy, was found to be excellent. R.S.D. values, determined in the framework of an extensive reproducibility study, ranged between 1.47 and 9.02%. Detection limits were in the low ng/L range for all compounds with linear ranges extending up to two orders of magnitude. Method accuracy was determined by analyzing a certified reference material (PH- 1JM), spiked water samples and participating in a series of round robin tests and did not reveal any significant bias for the different compounds under investigation.     

Observation of double ø-meson production in 100 and 175 GeV π−-Be interactions

Inclusive øø production has been studied in π^?-Be interactions for 100 and 175 GeV incident momentum. An upper limit of 72 nb has been set for $\text{σ(π}{}^{\mathrm{?}}\text{Be → η}{}_{\mathrm{<mtext>c</mtext>}}\text{(2980) +}\text{X}\text{)}\text{s}\text{?}\text{BR}\text{(η}{}_{\mathrm{<mtext>c</mtext>}}\text{→ øø) at 175 GeV}$. At both momenta the number of øø events is larger than expected for uncorrelated ø pairs. A narrow width enhancement is observed at M_øø≈2100 MeV with a 4 standard deviation significance.     

Quantity equations, rationalization and change of number of fundamental quantities II

Summary The experience gathered in a preceeding article, in which questions relating to the interpretation of quantity equations were elucidated by means of a simple example, is applied to some of the equations occurring in the field of electromagnetism, especially as regards rationalization.In a preceeding paper¹) (to be quoted as I) we have given a personal view regarding quantity equations and their interpretation. In the present article we shall make an attempt at applying these considerations to some of the equations occurring in the field of electromagnetism, especially as regards the rationalization of those equations by which the quantitiesH, D and are introduced or defined. To make comparison easy, the results obtained in I will be repeated in a condensed form, as far as necessary.     

Presence versus Proximity: The Role of Pendant Amines in the Catalytic Hydrolysis of a Nerve Agent Simulant

Amino‐functionalized zirconium‐based metal‐organic frameworks (MOFs) have shown unprecedented catalytic activity compared to non‐functionalized analogues for hydrolysis of organophosphonate‐based toxic chemicals. Importantly, the effect of the amino group on the catalytic activity is significantly higher in the case of UiO‐66‐NH₂, where the amino groups reside near the node, compared to UiO‐67‐m‐NH₂, where they are directed away from the node. Herein, we show that the proximity of the amino group is crucial for fast catalytic activity towards hydrolysis of organophosphonate‐based nerve agents. The generality of the observed amine‐proximity‐dictated catalytic activity has been tested on two different MOF systems which have different topology. DFT calculations reveal that amino groups on all the MOFs studied are not acting as Brønsted bases; instead they control the microsolvation environment at the Zr₆‐node active site and therefore increase the overall catalytic rates.     

Fraction auctions: The tradeoff between efficiency and running time

This paper studies the sales of a single indivisible object where bidders have continuous valuations. In Grigorieva et al. [14] it was shown that, in this setting, query auctions necessarily allocate inefficiently in equilibrium. In this paper we propose a new sequential auction, called the c-fraction auction. We show the existence of an ex-post equilibrium, called bluff equilibrium, in which bidders behave truthfully except for particular constellations of observed bids at which it is optimal to pretend a slightly higher valuation. We show c-fraction auctions guarantee approximate efficiency at any desired level of accuracy, independent of the number of bidders, when bidders choose to play the bluff equilibrium. We discuss the running time and the efficiency in the bluff equilibrium. We show that by changing the parameter c of the auction we can trade off efficiency against running time.     

Is the 7/2(1)- isomer state of 43S spherical?

We report on the spectroscopic quadrupole moment measurement of the 7/2(1)(-) isomeric state in (16)(43)S(27) [E*=320.5(5) keV, T(1/2)=415(3) ns], using the time dependent perturbed angular distribution technique at the RIKEN RIBF facility. Our value, |Q(s)|=23(3) efm(2), is larger than that expected for a single-particle state. Shell model calculations using the modern SDPF-U interaction for this mass region reproduce remarkably well the measured |Q(s)|, and show that non-negligible correlations drive the isomeric state away from a purely spherical shape.